HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231427Generated: October 26, 2026
Acetic Acid → N-[4-chloro-2-fluoro-5-(1-methoxyethyl)phenyl]-3,4,5,6-tetrahydrophthalimide
https://huagongshe.com/reaction/231427
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 3a,4,5,7a-Tetrahydro-2-benzofuran-1,3-dione | HCID 12726601 | — |
| Reactant | HCID 14501809 | HCID 14501809 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-[4-chloro-2-fluoro-5-(1-methoxyethyl)phenyl]-3,4,5,6-tetrahydrophthalimide | HCID 20032354 | 40.8% |
Reaction Steps
A mixture of 0.58 g (0.0029 mole) of 4-chloro-2-fluoro-5-(1-methoxyethyl)aniline, 0.82 g (0.0054 mole) of tetrahydrophthalic anhydride, and 15 ml of acetic acid was refluxed overnight. The acetic acid was then evaporated under reduced pressure, leaving a residue which was dissolved in diethyl ether. This solution was washed successively with water and an aqueous solution of sodium bicarbonate. The solution was dried, filtered, and the solvent was evaporated under reduced pressure leaving a residue. This residue was passed through a silica gel column, eluting with ethyl acetate/heptane (1/4). Appropriate fractions were combined, and the solvent was evaporated under reduced pressure, yielding 0.4 g of N-[4-chloro-2-fluoro-5-(1-methoxyethyl)phenyl]-3,4,5,6-tetrahydrophthalimide as a solid, m.p. 141°-44° C. The nmr and ir spectra were consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04846882 |
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| Source dataset | uspto-grants-1989_07 |
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| ORD ID | ord-4c216e5b822b4668ab93fedf00ba693d |
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| Source note | uspto-grants-1989_07 |
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